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Research output: Contribution to Journal/Magazine › Journal article › peer-review
Research output: Contribution to Journal/Magazine › Journal article › peer-review
}
TY - JOUR
T1 - Using highly time-resolved online mass spectrometry to examine biogenic and anthropogenic contributions to organic aerosol in Beijing
AU - Mehra, Archit
AU - Canagaratna, Manjula
AU - Bannan, Thomas J.
AU - Worrall, Stephen D.
AU - Bacak, Asan
AU - Priestley, Michael
AU - Liu, Dantong
AU - Zhao, Jian
AU - Xi, Weiqi
AU - Sun, Yele
AU - Hamilton, Jacqueline F.
AU - Squires, Freya
AU - Lee, James
AU - Bryant, Daniel J.
AU - Hopkins, James R.
AU - Elzein, Atallah
AU - Budisulistiorini, Sri Hapsari
AU - Cheng, Xi
AU - Chen, Qi
AU - Wang, Yuwei
AU - Wang, Lin
AU - Stark, Harald
AU - Krechmer, Jordan E.
AU - Brean, James
AU - Slater, Eloise
AU - Whalley, Lisa
AU - Heard, Dwayne
AU - Ouyang, Bin
AU - Acton, Joe
AU - Hewitt, C N
AU - Wang, Xinming
AU - Fu, Pingqing
AU - Jayne, John
AU - Worsnop, Douglas R.
AU - Allan, James
AU - Percival, Carl J.
AU - Coe, Hugh
PY - 2021/3/1
Y1 - 2021/3/1
N2 - Organic aerosols, a major constituent of fine particulate mass in megacities, can be directly emitted or formed from secondary processing of biogenic and anthropogenic volatile organic compound emissions. The complexity of volatile organic compound emission sources, speciation and oxidation pathways leads to uncertainties in the key sources and chemistry leading to formation of organic aerosol in urban areas. Historically, online measurements of organic aerosol composition have been unable to resolve specific markers of volatile organic compound oxidation, while offline analysis of markers focus on a small proportion of organic aerosol and lack the time resolutionto carry out detailed statistical analysis required to study the dynamic changes inaerosol sources and chemistry. Here we use data collected as part of the joint UK–China Air Pollution and Human Health (APHH-Beijing) collaboration during a field campaign in urban Beijing in the summer of 2017 alongside laboratory measurements of secondary organic aerosol from oxidation of key aromatic precursors (1,3,5-trimethylbenzene, 1,2,4-trimethyl benzene, propyl benzene, isopropyl benzene and 1-methyl naphthalene) to study the anthropogenic and biogenic contributions to organic aerosol.For the first time in Beijing, this study applies positive matrix factorisation to online measurements of organic aerosol composition from a time-of-flight iodide chemical ionisation mass spectrometer fitted with a filter inlet for gases and aerosols (FIGAEROToF-I-CIMS). This approach identifies the real-time variations in sources and oxidation processes influencing aerosol composition at a near-molecular level. We identify eight factors with distinct temporal variability, highlighting episodic differences in OA composition attributed to regional influences and in situ formation. These have average carbon numbers ranging from C5–C9 and can be associated with oxidation of anthropogenic aromatic hydrocarbons alongside biogenic emissions of isoprene, apinene and sesquiterpenes.
AB - Organic aerosols, a major constituent of fine particulate mass in megacities, can be directly emitted or formed from secondary processing of biogenic and anthropogenic volatile organic compound emissions. The complexity of volatile organic compound emission sources, speciation and oxidation pathways leads to uncertainties in the key sources and chemistry leading to formation of organic aerosol in urban areas. Historically, online measurements of organic aerosol composition have been unable to resolve specific markers of volatile organic compound oxidation, while offline analysis of markers focus on a small proportion of organic aerosol and lack the time resolutionto carry out detailed statistical analysis required to study the dynamic changes inaerosol sources and chemistry. Here we use data collected as part of the joint UK–China Air Pollution and Human Health (APHH-Beijing) collaboration during a field campaign in urban Beijing in the summer of 2017 alongside laboratory measurements of secondary organic aerosol from oxidation of key aromatic precursors (1,3,5-trimethylbenzene, 1,2,4-trimethyl benzene, propyl benzene, isopropyl benzene and 1-methyl naphthalene) to study the anthropogenic and biogenic contributions to organic aerosol.For the first time in Beijing, this study applies positive matrix factorisation to online measurements of organic aerosol composition from a time-of-flight iodide chemical ionisation mass spectrometer fitted with a filter inlet for gases and aerosols (FIGAEROToF-I-CIMS). This approach identifies the real-time variations in sources and oxidation processes influencing aerosol composition at a near-molecular level. We identify eight factors with distinct temporal variability, highlighting episodic differences in OA composition attributed to regional influences and in situ formation. These have average carbon numbers ranging from C5–C9 and can be associated with oxidation of anthropogenic aromatic hydrocarbons alongside biogenic emissions of isoprene, apinene and sesquiterpenes.
U2 - 10.1039/d0fd00080a
DO - 10.1039/d0fd00080a
M3 - Journal article
VL - 226
SP - 382
EP - 408
JO - Faraday Discussions
JF - Faraday Discussions
SN - 1359-6640
ER -